Congenital nongoitrous hypothyroidism 6

Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the THRA gene.

Also known as: CHNG6, THRA hypothyroidism, congenital, nongoitrous, hypothyroidism, congenital, nongoitrous caused by mutation in THRA, hypothyroidism, congenital, nongoitrous, 6, hypothyroidism, congenital, nongoitrous, type 6

1 clinical trial for this condition and its sub-types, 0 tagged with Congenital nongoitrous hypothyroidism 6 itself.